Wang, Hung-Li <br/><br/>
Functional analysis of connexin-32 mutants associated with X-linked dominant Charcot-Marie-Tooth disease.  [electronic resource] 

 -  Neurobiology of disease  Mar 2004 
 - 361-70 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0969-9961 
<br/><br/><label>Standard No.: </label>10.1016/j.nbd.2003.11.005  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Animals<br/>Axons--metabolism<br/>Cell Membrane--genetics<br/>Cells, Cultured<br/>Charcot-Marie-Tooth Disease--genetics<br/>Connexins--genetics<br/>Demyelinating Diseases--genetics<br/>Gap Junctions--genetics<br/>Genes, Dominant<br/>Genetic Diseases, X-Linked--genetics<br/>Humans<br/>Ion Channels--genetics<br/>Membrane Potentials--genetics<br/>Mice<br/>Mutation--genetics<br/>Patch-Clamp Techniques<br/>Schwann Cells--metabolism<br/>Gap Junction beta-1 Protein